This project has been built to provide a solid community standing in the UK for the people who live with Triple X Syndrome. This site aims to provide an overview of own support projects, other support networks available, information leaflets we've created, and available published research written by others. Furthermore, while we are working towards encouraging more research, we are not actively conducting any research. When that changes, details of how to take part will be listed on the main site page.
This is a self support group website. These views and opinions displayed here are based primarily on our lives and experiences of those living with Triple X syndrome or dealing with it. Although great care has been taken to ensure the accuracy of the information in this website, Triple X Syndrome Support, cannot accept responsibility for any errors or omissions. Any information on this website is provided for self-help/information purposes only and is not a substitute for personal, medical or genetic advice. Users should consult a medically qualified clinician in all matters relating to the management of their health. Triple X Syndrome Support mentions other organisations’ websites and networking information. The linked websites and contributions might represent other people’s opinions and experiences. This does not imply that we endorse their content or have any responsibility for it.
All intellectual and other property in the information contained in this site is held by Triple X Syndrome Support is subject to copy write. You may download or print copies of our leaflets, or other information contained within this site for your own private or professional non-commercial use only, provided that you do not change any copyright, or other proprietary notices; all other copying, reproducing, transmitting, distributing or displaying of material on this site (by any means and in whole or in part) without the written permission of Triple X Syndrome Support is prohibited.